Amoxicillin and Clavulanate Potassium Tablets USP recall: Subpotent
Amoxicillin and Clavulanate Potassium Tablets USP, Chewable 400mg/57mg, 20-count bottles, Rx only, Manufactured in Canada By: Teva Canada Limited…
Why was Amoxicillin and Clavulanate Potassium Tablets USP recalled?
Subpotent Drug
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 100047634 Exp. Date 4/2025; 35449379A, Exp. Date 7/2024
- Product
- Amoxicillin and Clavulanate Potassium Tablets USP, Chewable 400mg/57mg, 20-count bottles, Rx only, Manufactured in Canada By: Teva Canada Limited…
- Recalling firm
- Teva Pharmaceuticals USA, Inc
- Quantity
- 34,448 bottles
- Distribution
- Nationwide within the United States
- Recall date
- June 26, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)